Byrnes E M, Bruno J P
Department of Psychology, Ohio State University, Columbus 43210.
Dev Psychobiol. 1994 Sep;27(6):409-24. doi: 10.1002/dev.420270608.
The D1- and D2-mediation of stimulated motor behavior was studied in pups (Days 10-11) and weanlings (Days 20-21) that had been depleted of dopamine (DA) on postnatal Day 3. Administration of the D1-like agonist SKF 38393 (30.0 mg/kg) or the D2-like agonist quinpirole (3.0 mg/kg) increased the incidence of sniffing and locomotion in intact and DA-depleted animals tested at either age. However, the ability of selective DA antagonists to reduce these stimulated responses interacted with both the depletion and the age at the time of testing. When tested as pups, both the D1 antagonist SCH 23390 (0.2 or 0.4 mg/kg) and the D2 antagonist clebopride (10.0 mg/kg) suppressed the behaviors induced by either class of DA agonist. When tested as weanlings, intact animals exhibited the profile of pups (i.e., either antagonist blocked each agonist). In DA-depleted weanlings, however, only the D1 antagonist blocked the D1 agonist-induced responses and only the D2 antagonist blocked the D2 agonist-induced responses. These data demonstrate that the interactions between D1 and D2 receptors in the expression of stimulated motor behaviors are altered following DA depletions in neonates. Moreover, this change in receptor function occurs sometime between 7 and 13 days after the DA depletion.
研究了出生后第3天多巴胺(DA)耗竭的幼崽(10 - 11日龄)和断奶幼崽(20 - 21日龄)中,D1和D2对刺激运动行为的介导作用。给予D1类激动剂SKF 38393(30.0mg/kg)或D2类激动剂喹吡罗(3.0mg/kg),可增加在两个年龄段测试的完整动物和DA耗竭动物的嗅探和运动发生率。然而,选择性DA拮抗剂降低这些刺激反应的能力,与测试时的DA耗竭情况和年龄均存在相互作用。在幼崽阶段进行测试时,D1拮抗剂SCH 23390(0.2或0.4mg/kg)和D2拮抗剂氯波必利(10.0mg/kg)均能抑制两类DA激动剂诱导的行为。在断奶幼崽阶段进行测试时,完整动物表现出与幼崽相同的情况(即任何一种拮抗剂均可阻断每种激动剂)。然而,在DA耗竭的断奶幼崽中,只有D1拮抗剂能阻断D1激动剂诱导的反应,只有D2拮抗剂能阻断D2激动剂诱导的反应。这些数据表明,新生儿DA耗竭后,刺激运动行为表达中D1和D2受体之间的相互作用发生了改变。此外,这种受体功能的变化发生在DA耗竭后的7至13天之间的某个时间点。